Wärme-Pflaster Nacken Display

Organization name

Jiangsu Hanyao Medical Devices Co.,Ltd

SRN

CN-MF-000030482

Manufacturer status

Active

10 warnings recorded — scroll inside the panel to see all entries.

• Ask your pharmacist or doctor for advice before using or taking the product (e.g. if pregnant or breastfeeding)
• Consult healthcare professional before use
• Consult instructions for use
• Do not cut
• Do not re-use
• Do not use if package is damaged
• Do not use past indicated date
• Warning; Hot surface
• Warning: • For single use only. Do not reuse and Do not use while sleeping. • If the heat pad material is damaged or tom. • With medicated lotions, creams or ointments. • On areas of bruising or swelling that have occurred within 48 hours. • If you are not capable of applying and removing the wrap by yourself. • If you are bedridden or prone to skin ulcers. • On areas of the body where you can’t feel heat, and use with caution in elder aged 65 and over • Be more careful to use for older people or the people whose skin acceptance for heat is lower • Check skin frequently for signs of burns or blisters, please stop use if you found • Stop use and ask a doctor if you experience any discomfort, burning, swelling, rash or other changes in your skin • To lower the risk of low-temperature burn, pls do not place extra stress pressure • Immediately stop use and ask a doctor if you experience any discomfort, burning, swelling, rash or other changes in your skin.

  OTHER

• Contraindication: • Can't use for people who have diabetes, poor circulation or heart disease. • Can’t use for people with rheumatoid arthritis. • Can't use together with other forms of therapeutic heat, including electric heating. • Can't use of unhealthy, damaged or broken skin, or sensitive skin. • Can't use for people unable to remove the product, including children, infants, pregnant women, and some elderly. • Can't use for children 18 and under. • If your doctor does not recommend its use for you or your condition.

  OTHER

Primary placement in Spain; available across 7 countries total.

Trade name

Wärme-Pflaster Nacken Display

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

16971996066688

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

697199606004P7

Reference / catalog number

02-059

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

20

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 297 MU50
• 95 MU50

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• Z120602PHYSIOTHERAPY EQUIPMENT

• Class IIa medical devices in EUDAMED

No certificate specifically references this device's Basic UDI-DI.

Certificate health across this manufacturer's portfolio.